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ReliOn

FDA UDI

Class II (US FDA UDI)

by Walmart Stores

Identity

Trade Name
ReliOn FDA UDI
Generic Name
Intermittent electronic patient thermometer FDA UDI
Device Name
Up-Grade Thermometer FDA UDI
Model / Reference
UPG2WRO-FP-1_0 FDA UDI
Description
Up-Grade Thermometer FDA UDI

Identifiers

Primary DI / UDI-DI
00681131078214 FDA UDI
510(k) Number
K983887 FDA UDI
FDA Product Code
FLL FDA UDI
GMDN Term
Intermittent electronic patient thermometer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.2910 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Intermittent electronic patient thermometer

ReliOn by Walmart Stores — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intermittent electronic patient thermometer.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Walmart Stores

Sources (1)

  • FDA UDI 4e5497ea-c10c-4fde-b2ea-bb73c75cb81f 34 fields · synced May 29, 2026